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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 7590-7605 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A new iterative inversion scheme of atomic scattering data within the framework of functional sensitivity analysis is presented. The inversion scheme is based on the first order Fredholm integral equation δσ(θ)=∫∞0K(θ,R)δV(R)R2 dR, K(θ,R)≡δσ(θ)/δV(R), or symbolically, δσ=KδV, which relates infinitesimal functional changes in the elastic differential cross section δσ(θ) and in the underlying interatomic potential δV(R). This equation can be written equivalently, via integration by parts, as δσ(θ)=∫∞0K[n](θ,R) {Rn×δV(n)(R)}R2 dR, or δσ=K[n]{Rn×δV(n)}, under the a priori assumption that {R(2+n)×K[n](θ,R)×δV(n−1) (R)}||∞R=0=0. Here K[n](θ,R)≡−R−(2+n) ×∫R0K[n−1](θ,R') R'(1+n)dR', δV(n)(R) ≡(dn/dRn)δV(R), with n=0,1,2,..., and K[0](θ,R)≡K(θ,R).A choice of n corresponds to a particular level of additional stabilization inverting the scattering data. By invoking a least squares regularization procedure and singular system analysis, the new indirect inversion scheme solves the linear relation δσ=K[n]{Rn×δV(n)} and results in the approximate solution Rn×δV(n)(R), which can in turn be integrated, n times, to yield the potential correction δV(R). The new algorithm not only makes the inversion more stable and more efficient, but also increases the sensitivity of the large angle scattering data to the repulsive part of the potential, in comparison with a previous method that directly solves the relation δσ=KδV.For illustration, the model system He–Ne is considered at both low- and high-collision energies, relative to the well depth of the potential. It is found that the indirect method based on the linear relation δσ=K[2]{R2×δV(2)} can more accurately determine both attractive and repulsive parts, including a large section of classically forbidden region, of the potential than its direct counterpart. Furthermore, the indirect method allows for substantial deviations of the initial reference potential from final result, not only in well depth, but in range parameter and asymptotic behavior. Finally, these observations are not significantly dependent on the magnitude of the collision energy.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 2305-2314 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A general iterative inversion procedure based on functional sensitivity analysis is presented for determining the gas–surface interaction potential from low energy elastic scattering data. Formally, Tikhonov regularization, singular function analysis, and a recently developed exact transformation technique are implemented to render the inversion stable and efficient. Specifically, the simulation of helium scattering from a rigid periodic xenon monolayer on the graphite (0001) face is considered. It is found that the functional sensitivity densities of the diffraction intensities with respect to the He–Xe/C(0001) potential contain profound information, thus are invaluable in guiding the inversion of scattering data to yield the potential. Although, unequivocal determination of the full three-dimensional potential from the inevitably incomplete experimental data may be difficult, we demonstrate that simulated input data consisting of a finite number of polar scan specular intensities can be used to accurately recover the underlying He–Xe/C(0001) potential. The recovered potential has been obtained without imposing any explicit functional form on the potential per se. The resulting procedure is quite promising for treating real laboratory data.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 3940-3944 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The reproducing kernel Hilbert space (RKHS) method has been previously shown to be accurate and efficient in the construction of potential energy surfaces (PES) by interpolating fully gridded high level ab initio data. This paper extends the RKHS method to handle partially filled data calculated over arbitrarily shaped regions, while keeping nearly intact its accuracy and efficiency. The extension permits points or regions to be added to or removed from the grid as needed before doing expensive ab initio calculations, thus enabling the construction of RKHS PESs from the data distributions that are most likely to occur in practice. The utility of the new technique is demonstrated using data from the lowest global RKHS PES for the reaction O(1D)+H2, showing that ignoring the irrelevant regions of the PES does not adversely impact the accuracy of the surfaces if the relevant region is adequately sampled. © 2001 American Institute of Physics.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 3945-3948 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present in detail the construction procedure of two high quality global potential energy surfaces that have recently been used in quasiclassical and quantum dynamics studies for the reaction N(2D)+H2→NH+H. The procedure is based on the reproducing kernel Hilbert space method to interpolate high-level multireference configuration interaction ab initio calculations using augmented polarized triple zeta basis sets. A particular molecular coordinate system has been adopted to treat the nonadditive three body interaction as well as to guarantee the triangle inequalities of three molecular bond lengths and permutation symmetry of the two hydrogen atoms. A new radial reproducing kernel that remains finite at short distances while decaying to zero at large distances has been introduced, especially, for treating the molecule in the linear H–N–H configurations. Moreover, a robust procedure has been devised to handle the cusp in the two-body H2 interaction associated with the 1 A″ potential energy surface. The resulting surfaces are smooth, accurate, efficient to evaluate, exactly reproducing the input data upon which they are based and represent a significant improvement over previous surfaces for this reaction. © 2001 American Institute of Physics.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 116 (2002), S. 4124-4134 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A procedure based on the reproducing kernel Hilbert space (RKHS) interpolation method has been implemented to produce a globally smooth potential energy surface (PES) for the 1 A′ state of the S(1D)+H2 reaction from a set of accurate ab initio data, calculated at the multireference configuration interaction level with augmented polarized quadruple-zeta basis sets and arranged on a three-dimensional regular full grid in the Jacobi coordinates. The procedure includes removing a small number of questionable ab initio data points, implementing a recently developed technique for efficiently handling a partially filled grid, and adopting a sequence of regularizations for attaining additional smoothness. The resulting RKHS PES is analytic, first-order differentiable, and fast to evaluate. Quasiclassical trajectory calculations have been performed and compared with the results based on a recent hybrid PES obtained from a combination of the RKHS interpolation in the entrance channel and Murrell–Carter (MC)-type fitting in the exit channel from the same set of ab initio data. Comparisons with recent experimental measurements show improvement of the present RKHS PES over the existing hybrid RKHS-MC PES. The results demonstrate that the entrance channel Jacobi coordinates can still be a good candidate in sampling the full configuration space for reactive systems involving three atoms. © 2002 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 3960-3968 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An efficient procedure based on the reproducing kernel Hilbert space interpolation method is presented for constructing intermolecular potential energy surfaces (PES) using not only calculated ab initio data but also a priori information on long-range interactions. Explicitly, use of the reciprocal power reproducing kernel on the semiinfinite interval [0,∞) yields a set of exact linear relations between dispersion (multipolar) coefficients and PES data points at finite internuclear separations. Consequently, given a combined set of ab initio data and the values of dispersion (multipolar) coefficients, the potential interpolation problem subject to long-range interaction constraints can be solved to render globally smooth, asymptotically accurate ab initio potential energy surfaces. Very good results have been obtained for the one-dimensional He–He potential curve and the two-dimensional Ne–CO PES. The construction of the Ne–CO PES was facilitated by invoking a new reproducing kernel for the angular coordinate based on the optimally stable and shape-preserving Bernstein basis functions. © 2000 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 4052-4060 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: An inversion algorithm based on first-order functional sensitivity analysis and Tikhonov regularization is extended for the determination of multiple (diabatic) potentials from elastic and/or inelastic scattering data. Two methods of inversion are presented. In order to illustrate the methods, two-state and three-state models of the He++Ne system are employed in a simulated inversion, the former for the recovery of an entire potential matrix, and the latter to obtain multiple coupling elements, as well as to compare and contrast the two methods against each other. In the case of the two-state model, good agreement between the recovered and the model potentials is achieved if initial guesses for V11(r) and [V22(r)−V22(∞)] are within ±5% of the model, and those for the coupling element V12(r) are within ±10%, thus indicating that the method may be useful for the simultaneous refining of abinitio calculations and the determination of coupling potentials. For the three-state case, initial guesses differing from the model coupling potentials by as much as ±50% yield successful inversions using either method, therefore indicating that the procedure may be even more useful for the recovery of multiple coupling potentials.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 2023-2032 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A general iterative inversion algorithm based on first-order functional sensitivity analysis and Tikhonov regularization is extended for the determination of diabatic coupling potentials from inelastic scattering data. For simplicity, the two-state case is presented here, and it is assumed that the (diagonal) diabatic potentials are known. "Noisy'' and "noise-free'' numerically simulated data, calculated from model potentials for He++Ne and Li+I, are used to illustrate the method. Various coupling potential trial functions are used, ranging from a constant multiple of the model to a step function. For most cases, the important regions of the coupling potential (i.e., those regions which are most sensitive to the inelastic scattering data, including the region of crossing) are recovered to high precision within four to seven iterations. Those cases which show a small range for convergence may indicate a limit of the present algorithm, based solely on first-order functional derivatives, and the need to extend it to include higher-order terms.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 13447-13456 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 108 (1998), S. 1780-1793 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Experimental absorption spectral data from Q-branch line mixing in HCN, C2H2, and N2O are inverted to extract their respective relaxation W matrices. The formulation makes use of a general iterative inversion algorithm based upon first-order sensitivity analysis and Tikhonov regularization. The algorithm, previously applied to R-branch line mixing in HCN, is reformulated to explicitly require detailed balance for the real, off-diagonal W matrix elements. As with the HCN R-branch case, the W matrices recovered typically were found to describe line mixing much better than those derived from the fitting laws currently in use, and the inversion algorithm usually converged within just three iterations. © 1998 American Institute of Physics.
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